Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Ann Surg Oncol. 2024 Mar;31(3):1996-2007. doi: 10.1245/s10434-023-14696-6. Epub 2024 Jan 4.
Select patients with peritoneal metastases are treated with cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS/HIPEC). We assayed for intra- and interpatient drug response heterogeneity through testing of patient-derived tumor organoids (PDTOs).
PDTOs were generated from CRS/HIPEC patients from December 2021 to September 2022 and subjected to an in vitro HIPEC drug screen. Drug response was assessed with a cell viability assay and cleaved caspase-3 staining.
A total of 31 patients were consented for tissue collection. Viable tissue was harvested from 23, and PDTO generation was successful in 13 (56%). PDTOs were analyzed from six appendiceal, three colorectal, two small bowel, one gastric, and one adrenal tumor. Drug screen results were generated in as few as 7 days (62%), with an average time of 12 days. Most patients received mitomycin-C (MMC) intraoperatively (n = 9); however, in only three cases was this agent considered the optimal choice in vitro. Three sets of PDTOs were resistant (defined as > 50% PDTO viability) to all agents tested and two were pan-sensitive (defined as 3 or more agents with < 50% PDTO viability). In three patients, organoids were generated from multiple metastatic sites and intrapatient drug response heterogeneity was observed.
Both intra- and interpatient drug response heterogeneity exist in patients undergoing CRS/HIPEC for nongynecologic abdominal cancers. Caution must be used when interpreting patient response to chemotherapeutic agents based on a single site of testing in those with metastatic disease.
部分腹膜转移患者接受细胞减灭术和腹腔热灌注化疗(CRS/HIPEC)治疗。我们通过检测患者来源的肿瘤类器官(PDTO)来检测患者的内在和个体间药物反应异质性。
从 2021 年 12 月至 2022 年 9 月接受 CRS/HIPEC 的患者中采集肿瘤组织,生成 PDTO,并进行体外 HIPEC 药物筛选。通过细胞活力测定和切割 caspase-3 染色评估药物反应。
共有 31 名患者同意采集组织。23 名患者采集到了可用于检测的组织,其中 13 名(56%)成功生成了 PDTO。PDTO 分析来自 6 例阑尾肿瘤、3 例结直肠肿瘤、2 例小肠肿瘤、1 例胃肿瘤和 1 例肾上腺肿瘤。在 7 天内(62%)即可获得药物筛选结果,平均时间为 12 天。大多数患者在术中接受了丝裂霉素 C(MMC)治疗(n=9);然而,只有 3 例在体外被认为是最佳选择。有 3 组 PDTO 对所有检测药物均有抗性(定义为>50%PDTO 活力),2 组对所有药物均敏感(定义为 3 种或以上药物对 PDTO 活力的抑制率<50%)。在 3 名患者中,从多个转移部位生成了类器官,并观察到个体内药物反应的异质性。
在接受 CRS/HIPEC 治疗非妇科腹部癌症的患者中,存在个体内和个体间药物反应异质性。在转移性疾病患者中,基于单一部位的检测来解释患者对化疗药物的反应时必须谨慎。